Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs2890565
UTS2
0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs11085725
TYK2
0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs34551253
TRPM5
0.925 0.080 11 2415234 missense variant C/A;T snv 2.3E-02 2
rs1328142
TRPM3
1.000 0.040 9 70783498 intron variant C/A snv 0.21 1
rs540386
TRAF6
0.851 0.200 11 36503743 intron variant C/G;T snv 4
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs2071295
TNXB
0.925 0.120 6 32070923 intron variant C/T snv 0.25 2
rs2239689
TNXB
0.925 0.120 6 32062507 intron variant G/A snv 0.33 0.25 2
rs13239597
TNPO3 ; TPI1P2
0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 3
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs12534421
TNPO3
1.000 0.040 7 128984019 intron variant C/A snv 9.0E-02 1
rs36073657
TNPO3
1.000 0.040 7 129011468 intron variant C/T snv 9.0E-02 1
rs62478615
TNPO3
1.000 0.040 7 129044262 intron variant G/C snv 9.0E-02 1
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 5
rs4958880
TNIP1
0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 3